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“STORZ MEDICAL” Modulith SLX-F2 Lithotripter - Taiwan Registration 276e2a17cd0800ebd5138f3661978c58

Access comprehensive regulatory information for “STORZ MEDICAL” Modulith SLX-F2 Lithotripter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 276e2a17cd0800ebd5138f3661978c58 and manufactured by Storz Medical AG. The authorized representative in Taiwan is KINDMED CORPORATION.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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276e2a17cd0800ebd5138f3661978c58
Registration Details
Taiwan FDA Registration: 276e2a17cd0800ebd5138f3661978c58
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Device Details

“STORZ MEDICAL” Modulith SLX-F2 Lithotripter
TW: “斯拓茲”體外震波碎石機
Risk Class 2
MD

Registration Details

276e2a17cd0800ebd5138f3661978c58

Ministry of Health Medical Device Import No. 036140

DHA05603614004

Company Information

Switzerland

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology and urology

H5990 Extracorporeal shock wave lithotripsy

Imported from abroad

Dates and Status

Dec 20, 2022

Dec 20, 2027